11{62 -PGE{HD 2{B -Type compounds

ABSTRACT

Novel methods are disclosed for transforming PGA2 and 15 Beta PGA2 and their acetates, methyl esters, and acetate methyl esters to various prostanoic acids and esters of the PGE2 and PGF2 series. Some of the latter are novel and are useful for the same pharmacological purposes as PGE2 and PGF2 .

United States Patent Pike et al.

llfi-PGE -TYPE COMPOUNDS Inventors: John E. Pike; William P. Schneider,

both of Kalamazoo, Mich.

Assignee: The Upjohn Company, Kalamazoo,

Mich.

Filed: Oct. 3, 1973 Appl. No.: 403,094

Related US. Application Data Division 0f Ser. No. 159,478, July 2, 1971, Pat. No. 3,772,350, which is a continuation-in-part of Ser. No. 71,390, Sept. 11, 1970, abandoned.

US. Cl... 260/468 D; 260/211 R; 260/247.2 R; 260/268 R; 260/293.65; 260/326.2;

260/50l.l; 260/50l.15; 260/50l.l7; 260/501.2; 260/514 D June 17, 1975 [51] Int. Cl C07c 61/32; C07c 69/74 [58] Field of Search 260/468 D, 514 D [56] References Cited OTHER PUBLICATIONS Floyd et al., Tet. Letters, 3209, (1972).

Primary Examiner-Robert Gerstl Attorney, Agent, or Firm-Morris L. Nielsen [5 7 ABSTRACT 3 Claims, No Drawings 1 llfl-PGEz-TYPE COMPOUNDS CROSS REFERENCE TO RELATED APPLICATIONS This is a division of application Ser. No. 159,478, filed July 2, 1971, now US. Pat. No. 3,772,350, which is a continuation-in-part of our co-pending application Ser. No. 71,390, filed Sept. I1, 1970 now abandoned.

DESCRIPTION OF THE INVENTION Some of the derivatives of prostanoic acid are known as prostaglandins. One of those, prostaglandin E (PGE has the following formula:

Another, prostaglandin F a (PGF has the formula:

Still another, prostaglandin F (PGF has the formula:

In Formulas I to IV and in the formulas recited hereinafter in the specification and claims, broken line attachments to the cyclopentane ring indicate substituents in alpha configuration, i.e., below the plane of the cyclopentane ring. Heavy solid line attachments to the cyclopentanc ring indicate substituents in beta configuration, i.e., above the plane of the cyclopentane ring.

The side-chain hydroxy at C in Formulas II to IV is in S (alpha) configuration. That configuration is shown by attachment of said side-chain hydroxy to C15 with a dotted line and hydrogen with a heavy solid line. The alternative configuration for the side-chain hydroxy at C-l5 is known as R or epi (beta), and is shown when necessary by attachment of said side-chain hydroxy to C-l5 with a heavy solid line and hydrogen with a dotted line, thus A, H OH.

The prostaglandin corresponding to PGE (Formula II) but with the R or epi configuration at C-l5 will be designated l5B-PGE See Nature, 212, 38 (1966) for discussion of the stereochemistry of the prostaglandins.

These conventions regarding formulas, names, and symbols for derivatives of prostanoic acid apply to the formulas, names, and symbols given hereinafter in the specification and claims. When reference is made hereinafter to the compounds of Formulas II to IV, by the symbols PGE PGF or PGF p or to the methyl esters of any of those, 15(S) configuration will be intended and by established custom, S or alpha will not be mentioned in the name or symbol. For all of the other compounds recited hereinafter, the configuration at C-l5 will be identified in the name as 158 whenever the 15(R) configuration is intended.

Molecules of the known prostaglandins each have several centers of asymmetry, and can exist in racemic (optically inactive) form and in either of the two enantiomeric (optically active) forms, i.e., the dextrorotatory and levorotatory form As drawn, Formulas II to IV each represent the particular optically active form of the prostaglandin which is obtained from certain mammalian tissues, for example, sheep vesicular glands, swine lung, or human seminal plasma, or by carbonyl and/or double bond reduction of a prostaglandin so obtained. See, for example, Bergstrom et al., Pharmacol. Rev. 20, 1 (1968) and references cited therein.

The several aspects of this invention relate to novel methods for preparing PGE PGF and PFG their acetates and methyl esters, and the ISB-epimers of those compounds, to novel intermediates used in those methods, to novel methods used to make those intermediates, and to certain novel and pharmacologically useful analogs of PGE PGF and PGF B The novel and pharmacologically useful PGE PGF and PGF analogs of this invention have the formulas:

H OH H I j Or I In Formula V, B is ll :1 or H, 0%.

In Formula VI, indicates attachment to the ring in alpha or beta configuration.

It will be observed that each of the novel compounds of Formulas V and VI has ahydroxy group attached to the I l-position in beta configuration. In PGE PGF q and PGF and in the compounds of Formula VII, the hydroxy at C-l I is attached in alpha configuration.

With regard to Formulas V, VI, and VII, examples of alkyl of one to 8 carbon atoms, inclusive, are methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, and isomeric forms thereof. Examples of cycloalkyl of 3 to carbon atoms, inclusive, which includes alkylsubstituted cycloalkyl, are cyclopropyl, 2-methylcyclopropyl, 2,2-dimethylcyclopropyl, 2,3-diethylcyclopropyl, 2-butylcyclopropyl, cyclobutyl, 2- methylcyclobutyl, 3-propylcyclobutyl, 2,3,4-triethylcyclobutyl, cyclopentyl, 2,2-dimethylcyclopentyl, 3-pentylcyclopentyl, 3-tert-butylcyclopentyl, cyclohexyl, 4-tert-butylcyclohexyl, 3-isopropylcyclohexyl, 2,2-dimethylcyclohexyl, cycloheptyl, cyclooctyl, cyclononyL-and cyclodecyl. Examples of aralkyl of 7 to 12 carbon atoms, inclusive, are benzyl, phenethyl, I- phenylethyl, 2phenylpropyl, 4-phenylbutyl, 3- phenylbutyl, 2-( I -naphthylethyl), and 1-( 2- naphthylmethyl). Examples of phenyl substituted by one to 3 chloro or alkyl of one to 4 carbon atoms, inclusive, are p-chlorophenyl, m-chlorophenyl, ochlorophenyl, 2,4-dichlorophenyl, 2,4,6- trichlorophenyl, p-tolyl, m-tolyl, o-tolyl, p-ethylphenyl, p-tert-butylphenyl, 2,5-dimethylphenyl, 4-chloro-2- methylphenyl, and 2,4-dichloro-3-methylphenyl.

The known prostanoic acid derivatives, PGE PGF, and PGF and their esters and pharmacologically acceptable salts are extremely potent in causing various biological responses. For that reason, these compounds are useful for pharmacological purposes. See, for example, Bergstrom et al., cited above, and references cited therein. A few of those biological responses are systemic arterial blood pressure lowering in the case of the PGE and PGE3 compounds as measured, for example, in anesthetized (pentobarbital sodium) pentolinium-treated' rats with indwelling aortic and right heart cannular; pressor activity, similarly measured, for'the PGF compounds; stimulation of smooth muscle as shown, for example, by tests on strips of guinea pig ileum, rabbit duodenum, or gerbil colon; potentiation of other smooth muscle stimulants; antilipolytic activity as shown by antagonism of epinephrine-induced mobilization of free fatty acids or inhibition of the spontaneous release of glycerol from isolated rat fat'pads; inhibition of gastric secretion in the case of the PGE compounds-as shown in dogs with secretion stimulated by food or histamine infusion; activity on thecentral nervous system; controlling spasm andfacilitating breathing in asthmatic conditions; decrease of blood 'platelet adhesiveness as shown by platelet-to-glass adhesiveness, and inhibition of blood platelet aggregation and thrombus formation induced by various physical stimuli, e.g., arterial injury, and various biochemical stimuli, e.g., ADP, ATP, serotonin, thrombin, and collagen; and in the case of the PGE compounds, stimulation of epidermal proliferation and keratinization as shown when applied in culture to embryonic chick and rat skin segments.

Because of these biological responses, these known prostaglandins are useful to study, prevent, control, or alleviate a wide variety of diseases and undesirable physiological conditions in birds and mammals, including humans, useful domestic animals, pets, and zoological specimens, and in laboratory animals, for example, mice, rats, rabbits, and monkeys.

For example, these compounds, and especially the PGE compounds, are useful in mammals, including man, as nasal decongestants. For this purpose, the compounds are used in a dose range of about 10 pg. to about 10 mg. per ml. of a pharmacologically suitable liquid vehicle or as an aerosol spray, both for topical application.

The PGE and PGFa compounds are useful in the treatment of asthma. For example, these compounds are useful as bronchodilators or as inhibitors of mediators, such as SRS-A and Histamine which are released from cells activated by an antigen-antibody complex. Thus, these compounds control spasm and facilitate breathing in conditions such as bronchial asthma, bronchitis, bronchiectasis, pneumonia and emphysema. For these purposes, these compounds are administered in a variety of dosage forms, e.g., orally in the form of tablets, capsules, or liquids; rectally in the form of tablets, capsules, or liquids; rectally in the form of suppositories; parenterally, subcutaneously, or intramuscularly, with intravenous administration being preferred in emergency situations; by inhalation in the form of aerosols or solutions for nebulizers; or by insufflation in the form of powder. Doses in the range of about 0.01 to 5 mg. per kg. of body weight are used I to 4 times a day, the exact dose depending on the age, weight, and condition of the patient and on the frequency and route of administration. For the above use these prostaglandins can be combined advantageously with other antiasthmatic agents, such as sympathomimetics (isoproterenol, phenylephrine, ephedrine, etc); xanthine derivatives (theophylline and aminophyllin); and corticosteroids (ACTH and predinisolone). Regarding use of these compounds see South African Pat. No. 681,055.

The PGE compounds are useful in mammals, including man and certain useful animals, e.g., dogs and pigs, to reduce and control excessive gastric secretion, thereby reducing or avoiding gastrointestinal ulcer formation, and accelerating the healing of such ulcers already present in the gastrointestinal tract. For this purpose, the compounds are injected or infused intravenously, subcutaneousiy, or intramuscularly in an infusion' dose range about 0.1 ug'. to about 500 pg. per kg. of'body weight per minute, or in a total daily dose by injection or infusion in the range about 0.1 to about 20 mg. per kg. of body weight per day, the exact dose depending on the age, weight, and condition of the patient or animal, and on the frequency and route of administration.

The PGE PGF and PGF compounds are useful whenever it is desired to inhibit platelet aggregation, to reduce the adhesive character of platelets, and to remove or prevent the formation of thrombi in mammals, including man, rabbits, and rats. For example, these compounds are useful in the treatment and prevention of myocardial infarcts, to treat and prevent post-operative thrombosis, to promote patency of vascular grafts following surgery, and to treat conditions such as atherosclerosis, arteriosclerosis, blood clotting defects due to lipemia, and other clinical conditions in which the underlying etiology is associates with lipid imbalance or hyperlipidemia. For these purposes, these compounds are administered systemically, e.g., intravenously, subscutaneously, intramuscularly, and in the form of sterile implants of prolonged action. For rapid response, especially in emergency situations, the intravenous route of administration is preferred. Doses in the range about 0.005 to about 20 mg. per kg. of body weight per day are used, the exact dose depending on the age, weight, and condition of the patient or animal, and on the frequency and route of administration.

The PGE PGF a and PGF compounds are especially useful as additives to blood, blood products, blood substitutes, and other fluids which are used in artificial extracorporeal circulation and perfusion of isolated body portions, e.g., limbs and organs, whether attached to the original body, detached and being preserved or prepared for transplant, or attached to a new body. During these circulations and perfusions, aggregated platelets tend to block the blood vessels and portions of the circulation apparatus. This blocking is avoided by the presence of these compounds. For this purpose, the compound is added gradually or in single or multiple portions to the circulating blood, to the blood of the donor animal, to the perfused body portion, attached or detached, to the recipient, or to two or all of those at a total steady state dose of about 0.001 to mg. per liter of circulating fluid. It is especially useful to use these compounds in laboratory animals, e.g., cats, dogs, rabbits, monkeys, and rats, for these purposes in order to develop new methods and techniques for organ and limb transplants.

The PGE compounds are extremely potent in causing stimulation of smooth muscle, and are also highly active in potentiating other known smooth muscle stimulators, for example, oxytocic agents, e.g., oxytocin, and the various ergot alkaloids including derivatives and analogs thereof. Therefore PGE for example, is useful in place of or in combination with less than usual amounts of these known smooth muscle stimulators, for example, to relieve the symptoms of paralytic ileus, or to control or prevent atonic uterine bleeding after abortion or delivery, to aid in expulsion of the placenta, and during the puerperium. For the latter purpose, the PGE compound is administered by intravenous infusion immediately after abortion or delivery at a dose in the range about 0.01 to about 50 ,ug. per kg. of body weight per minute until the desired effect is obtained. Subsequent doses are given by intravenous, subcutaneous, or intramuscular injection or infusion during puerperium in the range 0.01 to 2 mg. per kg. of body weight per day, the exact dose depending on the age, weight, and condition of the patient or animal.

The PGE and P6P; compounds are useful as hypotensive agents to reduce blood pressure in mammals, including man. For this purpose, the compounds are administered by intravenous infusion at the rate about 0.01 to about 50 ,ug. per kg. of body weight per minute, or in single or multiple doses of about 25 to 500 pg. per kg. of body weight total per day.

The PGE PGA and PGF B compounds also increase the flow of blood in the mammalian kidney, thereby increasing volume and electrolyte content of the urine. Therefore, these compounds are useful in managing cases of renal disfunction, especially those involving blockage of the renal vascular bed. Illustratively, the compounds are useful to alleviate and correct cases of edema resulting, for example, from massive surface burns, and in the management of shock. For these purposes, the compounds are preferably first administered by intravenous injection at a dose in the range 10 to 1000 pg. per kg. of body weight or by intravenous infusion at a dose in the range 0.1 to 20 pg. per kg. of body weight per minute until the desired effect is obtained. Subsequent doses are given by intravenous, intramuscular, or subcutaneous injection or infusion in the range 0.05 to 2 mg. per kg. of body weight per day.

The PGE PGF and PGF compounds are useful in place of oxytocin to induce labor in pregnant female animals, including man, cows, sheep, and pigs, at or near term, or in pregnant animals with intrauterine death of the fetus from about 20 weeks to term. For this purpose, the compound is infused intravenously at a dose 0.01 to 50 pg. per kg. of body weight per minute until or near the termination of the second stage of labor, i.e., expulsion of the fetus. These compounds are especially useful when the female is one or more weeks post-mature and natural labor has not started, or 12 to 60 hours after the membranes have ruptured and natural labor has not yet started.

The PGF PGF B and PGE compounds are useful for controlling the reproductive cycle in ovulating female mammals, including humans and animals such as monkeys, rats, rabbits, dogs, cattle, and the like. For that purpose, PGE or PGF a for example, is administered systemically, e.g., intravenously, subcutaneously, and intravaginally, at a dose level in the range 0.001 mg. to about 20 mg. per kg. of body weight of the female mammal, advantageously during a span of time starting approximately at the time of ovulation and ending approximately at the next expected time of menses or just prior to that time. Additionally, expulsion of an embryo or fetus (abortion) is accomplished by similar administration of the compound during the first third of the normal mammalian gestation period.

As mentioned above, the PGE compounds are potent antagonists of epinephrine-induced mobilization of free fatty acids. For this reason, this compound is useful in experimental medicine for both in vitro and in vivo studies in mammals, including man, rabbits, and rats, intended to lead to the understanding, prevention, symptom alleviation, and cure of diseases involving abnormal lipid mobilization and high free fatty acid levels, e.g., diabetes mellitus, vascular diseases, and hyperthyroidism.

The novel Formula-V, VI, and -VII PGE PGF- and PGF B analogs of this invention each cause the biological responses described above for PGE PGF a and PGF respectively, and each of these novel compounds is accordingly useful for the abovedescribed corresponding purposes, and is used for those purposes in the same manner as described above.

PGE PGF and PGF and their esters and pharmacologically acceptable salts are all potent in causing multiple biological responses even at low doses. For example, PGE is extremely potent in causing vasodepression and smooth muscle stimulation, and is also potent as an antilipolytic agent. Moreover, for many applications, these known prostaglandins have an inconveniently short duration of biological activity. In striking contrast, the novel analogs of Formulas V, VI, and VII are substantially more specific with regard to potency in causing prostaglandin-like biological responses, and have a substantially longer duration of biological activity. Therefore, each of these novel prostanglandin analogs is surprisingly and unexpectedly more useful than one of the corresponding abovementioned known prostaglandins for at least one of the pharmacological purposes because it has a different and narrower spectrum of biological activity than the known prostaglandins, and therefore is more specific in its activity and causes smaller and fewer undesired side effects than when the known prostaglandin is used for the same purpose. Moreover, because of its prolonged activity, fewer and smaller doses of the novel prostaglandin analog can frequently be used to attain the desired result.

The novel Formula-V, VI, and l-Vll prostaglandin analogs are used as described above in free acid form in ester form, or in pharmacologically acceptable salt form. When the ester form is used, the alkyl esters are preferred, especially the alkyl esters wherein the alkyl moiety contains 1 to 4 carbon atoms, inclusive. Of those alkyl, methyl and ethyl are especially preferred for optimum absorption of the compound by the body or experimental animal system.

Pharmacologically acceptable salts of these prostaglandin analogs useful for the purposes described above are those with pharmacologically acceptable metal cations, ammonium, amine cations, or quaternary ammonium cations.

Especially preferred metal cations are those derived from the alkali metals, e.g., lithium, sodium and potassium, and from the alkaline earth metals, e.g., magnesium and calcium, although cationic forms of other metals, e.g., aluminum, zinc and iron, are within the scope of this invention.

Pharmacologically acceptable amine cations are those derived from primary, secondary, or tertiary amines. Examples of suitable amines are methylamine, dimethylamine, trimethylamine, ethylamine, dibutylamine, triisopropylamine, N-methylhexylamine, decylamine, dodecylamine, allylamine, crotylamine, cyclopentylamine, dicyclohexylamine, benzylamine, dibenzylamine, a-phenylethylamine, B-phenylethylamine, ethylenediamine, diethylenetriamine, and like aliphatic, cycloaliphatic, and araliphatic amines containing up to and including about 18 carbon atoms, as well as heterocyclic amines, e.g., piperidine, morpholine, pyrrolidine, piperazine, and lower-alkyl derivatives thereof, e. g. l-methylpiperidine, 4- ethylmorpholine, 1 -isopropylpyrrolindine, 2- methylpyrrolidine, 1,4-dimethylpiperazine, 2-

methylpiperidine, and the like, as well as amines containing water-solubilizing or hydrophilic groups, e.g.,

mono-, di-, and triethanolamine, ethyldiethanolamine, N-butylethanolamine, Z-amino-l-butanol, 2-amino-2- ethyl-1,3-propanediol, 2-amino-2-methyl- 1 -propanol, tris(hydroxymethyl)aminomethane, N- phenylethanolamine, N-(p-tert-amylphenyl)diethanolamine, galactamine, N-methylglucamine, N- methylglucosamine, ephedrine, phenylephrine, epinephrine, procaine, and the like.

Examples of suitable pharmacologically acceptable quaternary ammonium cations are tetramethylammonium, tetraethylammonium, benzyltrimethylammonium, phenyltriethylammonium, and the like.

As discussed above, these novel prostaglandin analogs are administered in various ways for various purposes; e.g., intravenously, intramuscularly, subscutaneously, orally, intravaginally, rectally, buccally, sublingually, topically, and in the form of sterile implants for prolonged action.

For intravenous injection or infusion, sterile aqueous isotonic solutions are preferred. For that purpose, it is preferred because of increased water solubility to use the free acid form or the pharmacologically acceptable salt form. For subcutaneous or intramuscular injection, sterile solutions or suspensions of the acid, salt, or ester form in aqueous or non-aqueous media are used. Tablets, capsules, and liquid preparations such as syrups, elixirs, and simple solutions, with the usual pharmaceutical carriers are used for oral or sublingual administration. For rectal or vaginal administration, suppositories, tampons, ring devices, and preparations adapted to generate sprays or foams or to be used for lavage, all prepared as known in the art, are used. For tissue implants, a sterile tablet or silicone rubber capsule or other object containing or impregnated with the substance is used.

The novel compounds of Formulas V, VI, and VII wherein R is other than hydrogen, i.e., the esters wherein R is alkyl of one to 8 carbon atoms, inclusive, cycloalkyl of 3 to 10 carbon atoms, inclusive, aralkyl of 7 to 12 carbon atoms, inclusive, phenyl, phenyl substituted with one to 3 chloro or alkyl of one to 4 carbon atoms, inclusive, are prepared from the corresponding acids of Formulas V, VI, and VII, i.e., wherein R is hydrogen, by methods known in the art. For example, the alkyl, cycloalkyl, and aralkyl esters are prepared by interaction of said acids with the appropriate diazohydrocarbon. For example, when diazomethane is used, the methyl esters are produced. Similar use of diazoethane, diazobutane, l-diazo-Z-ethylhexane, diazocyclohexane, and phenyldiazomethane, for example, gives the ethyl, butyl, 2-ethylhexyl, cyclohexyl, and benzyl esters, respectively.

Esterification with diazohydrocarbons is.carried out by mixing a solution of the diazohydrocarbon in a suitable inert solvent, preferably diethyl ether, with the acid reactant, advantageously in the same or a different inert diluent. After the esterification reaction is complete, the solvent is removed by evaporation, and the ester purified if desired by conventional methods, preferably by chromatography. It is preferred that contact of the acid reactants with the diazohydrocarbon be no longer than necessary to effect the desired esterification, preferably about 1 to about 10 minutes, to avoid undesired molecular changes. Diazohydrocarbons are known in the art or can be prepared by methods known in the art. See, for example, Organic Reactions, John Wiley & Sons, Inc., New York, N.Y., Vol.

8, pp. 389-394 (1954). An alternative method for esterification of the carboxyl moiety of the novel PGF- type or PGE-type compounds of Formulas V, VI, and VI] comprises transformation of the free acid to the corresponding silver salt, followed by interaction of that salt with an alkyl iodide. Examples of suitable iodides are methyl iodide, ethyl iodide, butyl iodide, isobutyl iodide, tert-butyl iodide, cyclopropyl iodide, cyclopentyl iodide, benzyl iodide, phenethyl iodide, and the like. The silver salts are prepared by conventional methods, for example, by dissolving the acid in cold dilute aqueous ammonia, evaporating the excess ammonia at reduced pressure, and then adding the stoichiometric amount of silver nitrate.

The phenyl and substituted phenyl esters of the formula-V, VI, and VII compounds are prepared by silylating the acid to protect the hydroxy groups, for example, replacing each OH with OSi(Cl-I Doing that may also change COOH to COO-Si- -(CH A brief treatment of the silylated compound with water will change COOSi--(CH back to -COOH. Procedures for this silylation are known in the art and are discussed hereinafter. Then, treatment of the silylated compound with oxalyl chloride gives the acid chloride which is reacted with phenol or the appropriate substituted phenol to give a silylated phenyl or substituted phenyl ester. Then the silyl groups, e.g., --O-Si(Cl-l are changed back to OH by treatment with dilute acetic acid. Procedures for these transformations are known in the art.

The novel Formula-V, VI, and VII acids (R is hydrogen) are transformed to pharmacologically accepatable salts by neutralization with appropriate amounts of the corresponding inorganic or organic base, examples of which correspond to the cations and amines listed above. These transformations are carried out by a variety of procedures known in the art to be generally useful for the preparation of inorganic, i.e., metal or ammonium salts, amine acid addition salts, and quaternary ammonium salts. The choice of procedure depends in part upon the solubility characteristics of the particular salt to be prepared. In the case of the inorganic salts, it is usually suitable to dissolve the acid in water containing the stoichiometric amount of a hydroxide, carbonate, or bicarbonate corresponding to the inorganic salt desired. For example, such use of sodium hydroxide, sodium carbonate, or sodium bicarbonate gives a solution of the sodium salt of the prostanoic acid derivative. Evaporation of the water or addition of a watermiscible solvent of moderate polarity, for example, a lower alkanol or a lower alkanone, gives the solid inorganic salt if that form is desired. I

To produce an amine salt, the acid is dissolved in a suitable solvent of either moderate or low polarity. Examples of the former are ethanol, acetone, and ethyl acetate. Examples of the latter are diethyl ether and benzene. At least a stoichiometric amount of the amine corresponding to the desired cation is then added to that solution. If the resulting salt does not precipitate, it is usually obtained in solid form by addition of a miscible diluent of low polarity or by evaporation. If the amine is relatively volatile, any excess can easily be removed by evaporation. It is preferred to use stoichiometric amounts of the less volatile amines.

Salts wherein the cation is quaternary ammonium are 7 produced by mixing the acid with the stoichiometric amount of the corresponding quaternary ammonium hydroxide in water solution, followed by evaporation of the water.

The novel compounds of Formulas V, VI, and VII wherein R, is hydrogen or methyl, i.e., the free acids and the methyl esters, and also PGE PGF and PGF B and the methyl esters of those are prepared by novel methods which are described hereinafter. For those methods, one of the following starting materials is used:

In Formulas Vlla, Vlll, and IX, R is either hydrogen or methyl, and R is hydrogen or acetyl.

It will be observed that the compounds encompassed by Formula Vlla are also encompassed by Vll. Thus, some Formula-VII compounds are useful both as intermediates and for pharmacological purposes.

These Formula-Vlla, VIII, and IX starting materials are all derivatives of prostanoic acid. The compounds of Formula Vlll are known in the art or are available by methods known in the art. See, for exam ple, Weinheimer et al., Tetrahedron Letters, No. 59, 5185 (1969); H. W. Youngken, Jr. (ed), Food-Drugs from the Sea", Proc. Marine Technology Society, pp. 311-314 (1969). The Formula-Vlll compound wherein R and R are both hydrogen is designated l5B-PGA alternatively l5(R)-PGA or l5-epi-PGA The other compounds encompassed by Formula Vlll are designated ISB-PGA; acetate, l5B-PGA methyl ester, and l5B-PGA acetate methyl ester.

The compounds of Formula Vlla are new in the art and methods for preparing them are described hereinafter. The Formula-Vila compound wherein R and R are both hydrogen is designated l5B-PGE alternatively l5(R)-PGE or IS-epi-PGE The other compounds encompassed by Formula Vlla are designated l5B-PGE l5-acetate. l5B-PGE methyl ester, and l5B-PGE acetate methyl ester.

The compounds of Formula lX are known in the art. See, for example, British Pat. Specification No. l,097,533. Novel methods for preparing these Formula-IX compounds are described hereinafter. The Formula-IX compound wherein R and R are hydrogen is designated PGA The other compounds encompassed by Formula lX are designated PGA acetate, PGA methyl ester, and PGA acetate methyl ester.

All of the compounds of Formulas Vlla, Vlll, and IX are obtained by extraction from a marine invertebrate. The compounds of Formula VlIa and Vlll, i.e., the 158 compounds, are obtained from colonies of Plexaura homomalla (Esper), 1792, forma R. The compounds of Formula lX, i.e., the 15(8) or alpha compounds, are

These Plexaura homomalla forms are members of the.

sub-class Octocorallia, order Gorgonaora, suborder Holaxonia, family Plexauridae, genus Plexaura. See, for example, Bayer, The Shallow-Water Octocorallia of the West Indian Region, Martinus Nijhoff, the Hague (1961). Colonies of these Plexaura homomalla forms are abundant on the ocean reefs in the zone from the lowtide line to about 25 fathoms in the tropical and subtropical regions of the western part of the Atlantic Ocean, from Bermuda to the reefs of Brazil, including the eastern shore reefs of Florida, the Caribbean island and mainland reefs, and the Gulf of Mexico island and mainland reefs. These colonies are bush-like or small tree-like in habit, and are readily identified for collection as Plexaura homomalla (Esper), 1792, by those of ordinary skill in this art. Forms R and S are distinguished by the methods describedin Preparation 1 below.

The colonies of these two forms of Plexaura homomalla are easily separated into an outer bark-like cortex and an inner wiry proteinaceous stem or skeleton. Symbiotic algae or Zooxanthellae are also present in the colonies. Weinheimer et'al., cited above, disclose the occurence of the Formula-VIII compounds wherein R and R are both hydrogen and wherein R is methyl and R is acetyl in the air dried cortex of Plexaura homomalla (Esper).

The choice of isolation or extraction method is determined by the particular Formula-VIIa, VIII, or -IX place.

The major component of fresh Plexaura homomalla (Esper), 1792, forma R is ISB-PGA acetate methyl ester, the Formula VIII compound wherein R is methyl and R is acetyl. Relatively minor components are the hydroxy methyl ester, the acetate, and the hydroxy acid of Formula VIII and the ISB-PGE compounds encompassed by Formula VIIa. Of the latter, the l5B-PGE acetate methyl ester (R is methyl and R is acetyl) is the most abundant. The major component of Plexaura homomalla (Esper), 1792, forms S is PGA acetate methyl ester, the Formula-IX compound wherein R is methyl and R is acetyl. Relatively minor components are the hydroxy methyl ester, the acetate, and the hydroxy acid of Formula IX, and the PGE compounds corresponding to Formula VIIa but having the (S) configuration. 1

When the acetate methyl ester compound of Formula VIIa, VIII, or IX (R is methyl, R is acetyl) is desired as a starting material, a suitable method comprises grinding the frozen whole Plexaura homomalla colonies or colony pieces, advantageously in a hogger to a particle size with the largest dimension about 5 'mm., and

then extracting the resulting particles with any of the usual organic solvents, preferably one with moderate to high polarity, e.g., dichloromethane or methanol, ad-

. mixer The desired compounds are isolated from the extract by evaporation, and then chromatography of the resulting residue. By this procedure, about 24 g. of ISB-PGA acetate methyl ester, and about one g. each of l5B-PGA methyl ester and l5B-PGE are obtained by dichloromethane extraction of 1500 g. of frozen Plexaura homomalla (Esper), 1792, forma R colonies or colony pieces. Similarly, relatively large amounts of PGA acetate methyl ester are obtained from frozen Plexaura homomalla (Esper), 1792, forma S.

when the l5-hydroxy methyl ester of Formula VIIa, VIII, or IX (R is methyl, R is hydrogen) is desired as a starting material, a suitable method comprises grinding the frozen whole Plexaura homomalla colonies or colony pieces as above, and then contacting the resulting particles with a lower alkanol, preferably methanol or ethanol, at 25C. for several days. The solvent is then evaporated and the residue chromatographed to give substantially larger amounts of the hydroxy methyl ester compound relative to the acetate methyl ester compound. When the contact between the Plexaura homomalla particles and the alkanol is substantially shorter, substantially the same amount and ratio of the various Formula-Vlla, VlII, or IX compounds is obtained with the alkanol as with dichloromethane. An alternative method for obtaining these l5-hydroxy methyl esters is descrbied below.

When 15B-PGA l5B-PGE or PGA (R and R in Formulas VIIa, VIII, and IX are both hydrogen) are desired as starting materials in the novel processes of this invention, they are prepared from the corresponding methyl esters and l5-acetate methyl esters after those have been extracted from the Plexaura homomalla colonies or colony pieces as described above. A suitable method for removing the acetyl group of each of the Formula-Vlla, VIII, and IX l5-acetate methyl esters comprises mixing the acetate methyl ester in lower alkanol solution, preferably in methanol solution, with a strong acid, e.g., perchloric acid, for about 15 hours at 25 C. A suitable method for removing the methyl group of any of the Formula-VIIa, VIII, and IX methyl esters is the enzymatic hydrolysis described in West Germany Offenlengungschrift No. 1,937,912, reprinted in Farmdoc Complete Specficiations, Book No. 14, No. 6869R, Week R Mar. 18, 1970.

Another method for obtaining l5B-PGA l5B-PGE or PGA from Plexaura homomalla colonies or colony pieces comprises freezing the Plexaura homomalla colonies or colony pieces, preferably at a temperature below about 20 C., and then allowing the colonies or colony pieces to thaw and warm to a temperature in the range 20 to 30 C. The thawed colonies or colony pieces are then maintained in the range 20 to 30 C. for at least 24 hours. After that treatment, substantially none of the Formula-VIIa, VIII, and IX compounds wherein R is methyl and R is acetyl are present, the principal Formula-VIIa, VIII, and IX compounds present being those wherein R and R are both hydrogen, the minor components being those wherein R is methyl and R is hydrogen or wherein R is hydrogen and R is acetyl. As before, Formula-Vlla and -VIII compounds are obtained from colonies of Plexdura homomalla (Esper), 1792, forma R, and Formula-IX compounds are obtained from col nies of Plexaura homomalla (Esper), 1 92, forma S.

A preferred procedure for the PGA and PGE type.

with the largest dimension about mm., and then maintaining the mixture in contact with water at a temperature in the range to C. for at least 24 hours. This mixture is filtered, and the filtrate is extracted with an appropriate water-immiscible solvent, e.g., ethyl acetate. The solid residue is also extracted with an appropriate solvent, e.g., methanol. The two extracts are evaporated, and the total residue is chromatographed to give Formula-Vlla and -VIII or Formula-IX compounds, the principal component in each case being the compound wherein R and R are both hydrogen.

Since our invention of the novel processes for transforming PGA and l5B-PGA and their methyl esters and acetate methyl esters to the various prostanoic acids and esters disclosed herein, it has now been found that small amounts of the 5,6-trans compounds of PGA and l5B-PGA and their methyl esters and acetate methyl esters are also obtained from Plexaura homomalla (Esper), 1792, forms R and S. These 5,6- Trans compounds are extracted with and accompany the corresponding PGA -type compounds through many of their transformations. For example, PGA containing 5,6-trans-PGA yields a' mixture of PGE and 5,6-trans-PGE by the process represented in Chart E below.

When it is desired, for pharmacological purposes, to prepare the major products of this invention free of 5,6-trans compounds, those 5,6-trans compounds are separated either from the starting reactants or from the products. In either case, several methods are available for separating the 5,6-trans-PG compounds from the PG compounds. One method is by means of a silversaturated ion-exchange resin (for example, see E. A. Emken et al., J. Am. Oil Chemists" Soc. 41, 388 (1964)), illustrated below in Preparations 5 and 6. The other method is by preferentially forming a mercuric acetate adduct of the 5,6-cis compound which is extractable into polar solvents illustrated below in Preparation 7.

Following the processes discussed herein and the procedures of the Examples below, the 5,6-trans-PG (and -l5,B-PG compounds are transformed to other 5,6-trans-PG (and -l5B-PG compounds, e.g., 5,6- trans-PGA to 5,6-trans-PGE 5,6-trans-l5B-PGA acetate methyl ester to 5,6-trans-l5B-PGF a acetate methyl ester, and the like.

As mentioned above, the Formula-Vlla, -VIII, and -IX compounds are starting materials for the preparation of PGE PGF and PGF the methyl esters of those, and also the novel compounds of Formulas V and VI, and some of the novel compounds of Formula VII. The novel processes using these starting materials will now be described.

The Formula-Vlll and -IX starting materials are both of the PGA-type. According to the novel processesof this invention, those are first transformed to corresponding PGE-type compounds. The chemical reactions involved in those transformations are shown generically in Chart A. i

In Chart A, R, is hydrogen, methyl, or Si(A) wherein A is alkyl of l to 4 carbon atoms, inclusive, aralkyl of 7 to 12 carbon atoms, inclusive, phenyl, or

phenyl substituted with one or 2 fluoro, chloro, or alkyl of one to 4 carbon atoms, inclusive; G is Pl 0R5 OI {\ORE,

wherein R is hydrogen, acetyl, or Si(A) when R,

is hydrogen ormethyl, and R is Si(A) when R, is -Si-(A) R is hydrogen or methyl; and B is n' bu Or bin Thus, Formula X in Chart A encompasses the starting materials of Formulas Vlll and IX obtained from Plexaura homomalla, and also compounds of the formula wherein R is as defined above, and Z is wherein A is as defined above. In Formula XI, of Chart A,

CHART A (oxidation) (reduction) 15 CHART A--Continued XI l (hydrolysis) XI I It will be observed in Chart A that the Formula-XII and -Xlll productseach encompass four stereoisomeric groups of compounds. Included are compounds with the 1 la,l5(S) configuration of PGE (Formula 1 1, above), compounds with the configuration of 1 101,153- PGE (Formula Vlla) as obtained from Plexaura homomalla (Esper), 1792, forma R, and both the 15(8) and 15(R) compounds with the NB configuration of the zoyel Formula v compounds of this invention wherein i.e.,l lB-PGE and l lB,l B-PGE If the Formula-XII or Xlll product is to have the (8) configuration, e.g., PGE or llB-PGE then the Formula-X starting material should have the 15(5) configuration, i.e., G should be if a 15/3 compound of Formula Xll or XIII is desired, e.g., l5[3-PGE or 1 1B,l5B-PGE then the Formula-X starting material should have the 15(R) or l5-epi configuration, i.e., G should be As described above, Formula-IX starting materials wherein R is hydrogen or methyl and R is hydrogen, and with the 15(8) configuration, are obtained from Plexaura homomalla (Esper), 1792, forma S. Those same compounds are also produced by, reacting the corresponding 15(R) (beta) compound with a hydrocarbyl or halohydrocarbyl sulfonyl chloride or brom de, preferably a lower alkylsulfonyl chloride or bromlde, especially methanesulfonyl chloride or bromide, or a benzeneor substituted-benzenesulfonyl chloride or bromide, e.g., p-toluenesulfonyl chloride. This reaction IS done in the presence of at least sufficient tertiary amine, e.g., triethylamine, to absorb the hydrogen chloride or hydrogen bromide by-product, and at a low temperature, preferably in the range l5 to +l5'C. The presence of an inert liquid diluent, e.g., tetrahydrofuran, is helpful to maintain a mobile homogenous reaction mixture. At 0 C. and with methanesulfonyl chloride, usually 30 to 60 minutes is a sufficient reaction time. The product is hydrolyzed to a mixture of 15(S) (alpha) and 15(R) hydroxy compounds. These are separated by procedures known in the art, and the l5(S) product is purified by procedures known in the art, advantageously by chromatography on silica gel. This reaction is also used to transform 15(S) FormulalX starting materials wherein R is hydrogen or methyl and R is hydrogen to the corresponding 15(R) compounds. In each case, a mixture of 15(R) product and 15(S) starting material is obtained,-the components of which are separated as described above.

Another method of transforming a l5B-PG compound to a PG compound is by converting it to a mixture of PG l5-formate and ISB-PG l5-formate compounds, separating the PG l5-formate, and hydrolyzing the PG l5-formate to the desired PG compound (see J. E. Pike et al., J. Org. Chem. 34, 3552 (1969)).

The mixture of alpha and beta l5-formates is prepared by maintaining the ISB compound, e.g. 15B- PGE l5B-PGA or l5B-PGF q in formic acid buffered with an alkali metal formate in the range 10 to C. until a substantial amount of the 153 compound, eg l5B-PGE 15-formate, has been transformed to the PG l5-formate. The mixture of the PG l5-formate and 15,8 l5-formates thus obtained is then separated by known methods, e.g. by chromatography.

The PG l5-formate can then be hydrolyzed to the desired PG l5-hydroxy compound. The l5B-PG l5- formate yields the corresponding l5/3-PG l5-hydroxy compound, which is then recycled through the above steps for further isomerization to the PG compound if desired.

This procedure is also useful to transform a PG compound to a 153 PG compound, by obtaining a mixture of the intermediate PG l5-formate and ISB-PG l5- formate compounds, separating them, and hydrolyzing them to the respective PG l5 hydroxy and ISB-PG l5- hydroxy compounds. In this case, the PG compound is recycled for further isomerization to the 153 compound.

Referring again to Chart A, the transformation of starting material X to epoxide Xl is carried out by reacting X with any agent known to epoxidize an afi-unsaturated ketone without reacting with isolated carboncarbon double bonds, for example see Steroid Reactions, Carl Djerassi, ed., Holden-Day Inc., 1963, p. 593. Especially preferred are aqueous hydrogen peroxide or an organic tertiary hydroperoxide. See, for example,

Organic Peroxides, A. V. Tobolsky et al., lnterscience Publishers, N.Y., For this purpose, the peroxide or hydroperoxide is employed in an amount of at least one equivalent per mole of Formula-X reactant in the presence of a strong base, e.g., an alkali metal hydrox- 17 and}; the like. See, for example, Sidgwick, Organic Chemistry of Nitrogen, Third Edition, rev. by Miller andufipiringall, Oxford, 1966, pp. 116-127.

1 The ratio of alpha to beta epoxide formed in the reaction is related to four factors: the epoxidizing agent, the base, the diluent, and the temperature. Hydrogen peroxide is employed in the concentrations usually available, for example 3 to 90%, although 30% is especially convenient. When the alpha epoxide is the desired product, tert-butyl hydroperoxide is especially preferred as the epoxidizing agent. Examples of other organic tertiary hydroperoxides useful for this purpose are tert-pentyl hydroperoxide, decahydronaphthyl hydroperoxide, oatx-dimethylbenzyl hydroperoxide, and 1,1-diphenylethyl hydroperoxide. The base is present in the proportion of 0.1-3.0, preferably about 0.1-0.5 equivalent of base per mole of starting material X when R., is methyl and R is acetyl; preferably about 1.5-2.5 equivalent of base per mole of starting material V111 or IX wherein R and R are hydrogen. When the alpha epoxide is the desired product, lithium hydroxide, lithium or magnesium alkoxides of one to 8 carbon atoms, and benzyltrimethylammonium hydroxide are the preferred bases, although the lithium and magnesium compounds are especially preferred.

It is advantageous to use an inert liquid diluent in the epoxidation step to produce a mobile homogenous reaction mixture, for example, a lower alkanol, dioxane, tetrahydrofuran, dimethoxyethane, dimethylsulfoxide, or dimethylsulfone. When the alpha epoxide is preferred, tetrahydrofuran or the less polar dimethoxyethane are especially preferred as the diluent. A reaction temperature in the range 60 to C. is generally preferred, especially below -l0 C. The lower temperatures below 30 C. are especially preferred for favoring formation of alpha epoxide over beta epoxide. At a temperature of 20 C., the epoxidation is usually complete in 3 to 6 hours. It is also preferred that the reaction be carried out in an atmosphere of an inert gas, e.g., nitrogen, helium, or argon. When the reaction is complete as shown by the absence of starting material as TLC plates (3% acetone in dichloromethane), the reaction mixture is neutralized, and the epoxy product is isolated by procedures known in the art, for example, evaporation of the diluent and extraction of the residue with an appropriate water-immiscible solvent, e.g., ethyl acetate.

This transformation of X toXl usually produces a mixture of Formula-X1 alpha and beta epoxides both with either the 15(R) or 15(8) configuration depending on the configuration at C-1 in the Formula-X starting material. Although these mixtures are separated into the individual alpha and beta isomers, for example, by chromatography by procedures known to be useful for separating alpha and beta epoxide mixtures, it is usually advantageous to transform the Formula-X1 mixture of alpha and beta epoxides to the corresponding mixture of Formula-X11 1 la and l 1,8 hydroxy compounds. The latter mixture is then readily separated into the 1 1a and 1 13 compounds, for example, by chromatography of silica gel.

During the transformation of epoxides X1 to alcohols Xll, an alpha epoxide yields an 1 la-hydroxy compound, and a beta epoxide yields an 1 lB-hydroxy compound. The ratio of alpha to beta epoxides in X1, and hence the eventual ratio of 11a and 11B alcohols in 18 XII, produced from starting material X is dependent in large measure on the nature of R in X. Recall that G is defined as ii 0?. mn or,

wherein R is hydrogen, acetyl, or -Si(A) wherein A is as defined above. For either definition of G, i.e., R configuration or S configuration, when R is hydrogen, more Formula-X1 beta epoxide is formed than when R is acetyl, and more Formula-X1 beta epoxide is formed when R is acetyl than when R is Si-(A) For example, when G in formula X is H OH,

the preferred basic hydrogen peroxide epoxidation gives about equal amounts of alpha and beta epoxides, but when G in formula X is about 3 parts of alpha epoxide and one part of beta epoxide are obtained, and when G in formula X is about 4 parts of alpha epoxide and one part of beta epoxide are obtained, both reactions with the same epoxidation reagent. When Gin formula X is about one part of alpha epoxide and 3 parts of beta epoxide are obtained with basic hydrogen peroxide, but when G is about 6 parts of alpha epoxide and 4 parts of beta epoxide are obtained with the same epoxidation reagent.

Each of the novel Formula-V and -VI compounds of this invention has a hydroxy attached in beta configuration to the cyclopentane ring. Some of the compounds of Formula V, i.e., when Y is i. n on m n on.

with the natural 1 1a configuration for the hydroxy at C-1 1 is the desired final product, e.g., PGE PGF a or PGF there is advantage in choosing a Formula- X starting material which gives a greater amount of the alpha epoxide during the transformation of X to XI. Those would be Formula-X compounds wherein X is 1i t =';U1.H-. or 11 -5; (A)

or the corresponding 15(S) compounds As mentioned above, the starting materials of Formula X encompass not only the Formula-VIII and -IX compounds obtained from Plexaura homomalla but also the silyl compounds of Formula Xa. When desired as reactants, these silyl compounds are prepared by silylation of PGA lB-PGA or the methyl esters of those. These silylations are carried out by procedures known in the art. See, for example, Pierce, Silylation of Organic Compounds, Pierce Chemical Co., Rockford, Ill. (1968). The C- hydroxy group of PGA l5B-PGA or their methyl esters is transformed to an OSi (A) moiety wherein A is as defined above, sufficient silylating agent being used according to known procedures to accomplish that. The necessary silylating agents for this purpose are known in the art or are prepared by methods known in the art. See, for example, Post, Silicones and Other Organic Silicon Compounds, Reinhold Publishing.Corp., New York, NY. (1949), In the case of PGA and ISB-PGA excess silylating agent and prolonged treatment also transform the COOH to COOSi(A) it is optional in transforming X to XI whether or not this COOl-l of PGA or ISB-PGA is esterified to COO Si-(A) since that ester group is transformed to f'COOl-l during formation and isolation of the Formula-XI epoxide product.

The various As ofa -Si-(A) are alike or different. For example, an Si-(A) can be trimethylsilyl, dimethylphenylsilyl, or methylphenylbenzylsilyl.

When it is desired to retain the Si(A) moiety at C15 in the Formula-X1 epoxide product, for example, to give steric control in a subsequent reaction, it is important in isolating the epoxide that the presence of acid be avoided and that contact with water be minimized unless the water is kept cold, i.e., below about 10 C.

Referring again to Chart A, the transformation of epoxide Xl to hydroxy compound XIl is accomplished by reduction with chromium (ll) salts, e.g., chromium (II) chloride or chromium (II) acetate. Those salts are prepared by methods known in the art, e.g., Inorganic Syntheses, VIII, 125 (1966); ibid., Vl, 144(1960); ibid. 111, 148 (1950); ibid. l, 122 (1939); and references cited in those. This reduction is carried out by procedures known in the art for using chromium (ll) salts to reduce epoxides of aB-unsaturated ketones to B-hydroxy ketones. See, for example, Cole et al., J. Org. Chem. 19, 131 (1954), and Neher et al., Helv. Chem. Acta 42, 132 (1959). In these reactions, the absence of air and strong acids is desirable. If it is desired to maintain a Si-(A) moiety on C-l5, a neutral reaction mixture is preferred. An especially preferred procedure is to generate the chromium (II) ion in the presence of the Formula-l epoxide, for example, by mixing the epoxide with a chromium (lll) salt, e.g., the chloride, with me-' tallic zinc in the presence of acetic acid. The desired Formula-XII compound is isolated from the reduction reaction mixture by methods known in the art, care being taken to minimize contact of the product with" acid and water, especially warm water, when retention of a Si(A) at C-l5 is desired.

Unexpectedly, amalgamated aluminum metal has also been found to be useful as a reducing agent in place of chromium (II)) salts to transform Formula XI epoxides to Formula XII hydroxy compounds. This reagent was previously not known to be useful for this type of reaction. This use of amalgamated aluminum represents a distinct and separate aspect of this invention.

Amalgamated aluminum is prepared by procedures known in the art, for example, by contacting aluminum metal in the form of foil, thin sheet, turnings, or granules with a mercury (1]) salt, for example, mercuric chloride, advantageously in the presence of sufficient water to dissolve the mercury (ll) salt. Preferably, the surface of the aluminum metal is free of oxide. That is readily accomplished by physical removal of the usual oxide layer, e.g., by abrasion or scraping, or chemically, e.g., by etching with aqueous sodium hydroxide solution. It is only necessary that the aluminum surface be amalgamated. The amalgamated aluminum should be freshly prepared, and maintained in the absence of air and moisture until used.

The reductive opening of the Formula-XI epoxide ring is accomplished by contacting said epoxide with the amalgamated aluminum in the presence of a hydroxylic solvent and sufficient inert organic liquid diluent to give a mobile and homogeneous reaction mixture with respect to the hydroxylic solvent and said epoxide. Among hydroxylic solvents, water is especially preferred although lower alkanols, e.g., methanol and ethanols are also operable.

Examples of inert organic liquid diluents are normally liquid ethers such as diethyl ether, tetrahydrofuran, dimethoxyethane, diglyme (dimethyl ether of diethylene glycol), and the like. Especially preferred is tetrahydrofuran. When a water-immiscible liquid diluent is used, a mixture of water and methanol or ethanol is especially useful in this reaction since the latter two solvents also aid in forming the desired homogeneous reaction mixture. For example, a mixture of diethyl ether and water is used with sufficient methanol to give a homogeneous reaction mixture.

This reductive opening requires two hydrogen atoms per molecule of epoxide. Amalgamated aluminum reacts readily with water and more slowly with other hydroxylic solvents to give hydrogen. One atomic equivalent of aluminum required 3 molecular equivalents of the hydroxylic solvent to give 3 atomic equivalents of hydrogen. Therefore, 1 molecular equivalent of epoxide requires two-thirds atomic equivalent of aluminum and 2 molecular equivalents of the hydroxylic solvent. Evolution of hydrogen gas (H molecules) is observed during this reductive opening of the epoxide. It is not known whether the reductive'opening is caused by hydrogen atoms or hydrogen molecules. However, some of the hydrogen gas escapes from the reaction mixture. Therefore, it is preferred to use an excess of amalgamated aluminum and hydroxylic solvent, preferably at least one atomic equivalent of aluminum and 3 molecular equivalents of hydroxylic solvent per molecular equivalent of epoxide. Because of the relatively high economic value of the epoxide compared with amalgamated aluminum and hydroxylic solvents, it is preferred to assure maximum yields of the desired Formula-XII hydroxy compound by use of substantially greater excess of amalgamated aluminum and hydrox: ylic solvent, e.g., up to times or more of those reagents than is theoretically required.

The reductive opening of the epoxide is carried out by mixing a solution of the epoxide in the organic diluent with the amalgamated aluminum and the hydroxylic solvent. Since the reaction is exothermic, it is usually advantageous to cool the solution to a low temperature, e.g., -20 C. to 0 C., before adding the amalgamated aluminum and hydroxylic solvent and to maintain the reaction mixture in the range 20 to 30 C, by external cooling. This is especially advantageous when water is used as the hydroxylic solvent. Higher reaction temperatures are operable but not preferred when a high yield of the Formula-XII products is desired. Stirring is preferred during the reaction since the reaction mixture is heterogeneous with respect to the solution and the amalgamated aluminum.

For reasons not understood, better yields and a shorter reaction time are usually observed when only part of the amalgamated aluminum is added at the start of the reaction, additional portions being added during the reaction, e.g., at one-hour intervals, than when the entire amount of amalgamated aluminum is added at the start of the reaction. A suitable procedure is to add about one-third of the amalgamated aluminum at the start, about one-third after 1 hour, and another third after a second hour. The course of the reaction is advantageously determined by withdrawing small portions of the solution and determining the presence or absence of starting material by thin layer chromatography. For example, when R is methyl and G is formula Xla wherein G and are as defined above and R is a cation of an alkali or alkaline earth metal or a quaternary ammonium group.

T hus,-the Formula-XI epoxide compound is treated with a hydroxide or oxide of lithium, sodium, potassium, magnesium, calcium, barium, or strontium prior to contacting with the aluminum amalgam. Optionally, the quaternary ammonium bases are used for this neutralization, for example benzyltrimethylammonium hydroxide. The base is used in equivalent amount to the acid so that R is replaced by the corresponding metal or quaternary ammonium cation. Alternatively, instead of the hydroxides or oxides, there are employed the hydrides, the carbonate, the bicarbonates, or the alkoxides, for example lithium hydride, potassium carbonate, sodium bicarbonate, magnesium methoxide, and the like, which form the corresponding Formula-Xla salts with the Formula-XI free acid. Alternatively, a metal or quaternary-ammonium carboxylate compound or .Formula-Xla salt carried forward from the epoxidation step, whether isolated in that step or not, is employed in the reductive step with aluminum amalgam. It is preferred that the Formula-Xla salt be soluble in the organic diluentalkanol-water or organic diluentwater medium used for the reduction step. By using the above-described salts, the reduction step proceeds smoothly without formation of insoluble aluminum salts which hinder the reaction. Following the reduction or hydrolysis step, the R cations are replaced with hydrogen by means known in the art, for example by acidification and extraction of the acid compound into an organic phase.

The desired Formula-XII hydroxy products are isolated by filtration of the reaction mixture, advantageously after addition of magnesium sulfate as a filter aid, and evaporation of the organic diluents. The Formula-XII products are then hydrolyzed if desired to remove Si(A) from C-l5, and the Ila and H5 products of Formula XIII are separated, if desired, by procedures known in the art, e.g., chromatography on silica gel.

The products of Formula-XII are all of the PGE -type and include-PGE PGE l5-acetate, PGE methyl ester, PGE l5-acetate methyl ester, PGE and PGE methyl ester with an OSi(A) at C- l 5, the corresponding 15, 3 compounds, and compounds corresponding to all of those wherein hydroxy is attached to C-ll in beta configuration.

As mentioned above, the transformation of X to XI to XII usually gives a mixture of Formula-XII PGE-type products, part with alpha and part with beta configuration for the hydroxy at C-1 1. There are several alternatives regarding that mixture. If O--Si-(A) is attached to C-lS, that can readily be transformed by hydrolysis to Ol-I. These hydrolyses are carried out by prior art procedures known to be useful for transforming silyl ethers to alcohols. See, for example, Pierce, cited above, especially p. 447 thereof. A mixture of water and sufficient of a water-miscible organic diluent to give a homogeneous hydrolysis reaction mixture represents a suitable reaction medium. Addition of a catalyticamount'of an organic or inorganic acid hastens the hydrolysis. The length of time required for the hydrolysis is determinedinpart ,by the hydrolysis temperature. With amixture of water and methanol at 25 C., several hours is usually sufficient for hydrolysis. At 0 C., several days is usually necessary. Also, if -OCOCl-I is attached to C-l5, that can readily be transformed to OH by acid-catalyzed alcoholysis as described above for removing the acetyl group of the Formula-VIlI and -IX PGA type starting materials. Both of those transformations are shown in Chart A, i.e., XII to XIII. Either before or after those transformations of XIItoXIII, the Formula-XII or XIII mixture of Ila and IIB isomers can be separated by methods known in the art, advantageously by chromatography on silica gel.

Further regarding the Formula-XIII compounds, those compounds wherein the configuraticn of the hydroxy at C-l l is beta are within the scope of the-Formula-V novel compounds of this invention, and those compounds wherein the configuration of the hydroxy at C-l I is alpha and B is are within the scope of the Formula-VII novel compounds of this invention. Both groups of novel compounds are used for pharmacological purposes described above for those compounds, the acids also being useful as reactants to prepare pharmacologically useful esters and pharmacologically acceptable and useful salts, both as described above. Moreover, Formula-XIII compounds wherein the configuration of the hydroxy at G1 I is alpha and B is l( on are PGE and PGE methyl ester, both of known pharmacological utility.

Still further regarding the separated compounds of Formulas XII and XIII, when a compound with one configuration at C-l l either alpha or beta, is desired as an intermediate or for pharmacological purposes, the other isomer is readily dehydrated to give additional Formula-X PGA-type starting material which is then used as a starting material according to the processes defined in Chart A and procedures described above to give additional of the desired isomer. These dehydrations are accomplished by procedures known in the art for dehydration of PGE-type compounds to PGA-type compounds. See, for example, Pike et al., Proc. Nobel Symposium II, Stockholm (1966), Interscience Publishers, New York, p. 162 (1967), and British Pat. Specification No. 1,097,533. These are acidic dehydrations, and alkanoic acids of 2 to 6 carbon atoms, inclusive, especially acetic acid, are preferred for this purpose. Dilute aqueous solutions of mineral acid, e.g., hydrochloric acid, especially in the presence of a solubilizing diluent, e.g., tetrahydrofuran, are also useful as reagents for these acidic dehydrations, although these reagents may also cause partial hydrolysis of the Formula- XII or -XIII methyl esters to carboxylic acids. A -Si(A) moiety at C-l5 is also removed during all of these acidic dehydrations.

Still further regarding the Formula-XII and -XIII compounds, either as mixtures or separately, any of those is transformed to other useful compounds or mixtures by changing these PGE-type compounds to PGF- type products by reducing the ring carbonyl at G9 to alpha hydroxy or beta hydroxy. Those transformations are shown in Chart B.

In Chart B, R, is hydrogen, methyl, or Si-(A) R is hydrogen or methyl, R, is hydrogen or Si-'(A) and G is H on, or H on,

wherein R is hydrogen or -Si-(A) when R, and R are hydrogen; R is hydrogen, acetyl, or Si(A) when'R 'and R are methyl; and R is Si-(A);, when R, is Si(A) wherein A is as defined above, with the proviso that when R is -Si(A) R is also -Si- --(A) Further in Chart B, B in Formula XVI is CHART i3 {si lylation.

6 XIV (reduction) y lysis or alcoholysisl XVI lB-PGE acetate, l5B-PGE methyl ester, and B- PGE methyl ester acetate are obtained from Plexaura homomalla (Esper), 1792, forma R. All of those compounds are encompassed by Formula XII, and thus, extraction of this form of Plexaura homomalla provides an alternative source of these starting materials.

Referring to Chart B, the starting material XII can be a mixture of compounds with regard to the configuration of C-] l, or the starting material can be stereochemically pure with respect to C-l 1, depending upon whether there has been an earlier separation of Ila and H13 isomers (see above discussion of Chart A reactions).

The transformation of PGE-type starting material XII to PGF-type product XVI involves reduction of a ring carbonyl to a ring hydroxy. This process is known in the art for some of the compounds encompassed by Formula XII, i.e., when the configuration at C-1 1 is alpha and the configuration at C-l5 is S. For the other compounds encompassed by Formula XII, this reaction is novel, and novel Formula-XV and -XVI compounds are produced.

For this carbonyl-to-hydroxy reduction, methods known in the art are used. See, for example, Pike et al., J. Org. Chem. 34, 3552 (1969). Use is made of any of the known ketonic carbonyl reducing agents which do not reduce ester or acid groups or carbon-carbon double bonds. Examples of those are the metal borohydrides, especially sodium, potassium, lithium, and zinc borohydrides, lithium (tri-tert-butoxy) aluminum hydride, meta trialkoxy borohydrides, e.g., sodium trimethoxyborohydride, and diisobutylaluminum hydride. The sodium, potassium, and zinc borohydrides are preferred for this reduction, especially zinc borohydride.

Unexpectedly, the amalgamated aluminum metal found useful above in transforming the Formula-XI epoxides to Formula-XII hydroxy compounds has also been found useful as an agent for this carbonyl-tohydroxy reduction of PGE-type compounds to PGF- type compounds. Either the PGE-type salts or the PGE- type esters are employed, for example the Formula-XII hydroxy compounds produced from the Formula-XI epoxides with or without intermediate isolation. Furthermore, the Formula-XI epoxides may be subjected to the combined epoxide'reduction and carbonylreduction reactions practically simultaneously by operating at higher temperatures, for example 4060 C., although it is preferred for high yields of the 11- hydroxy compounds that the reductions be done stepwise. The solvents which are operable for this reduction are generally the same as those found useful for the epoxide-reduction step. Somewhat higher temperatures or longer reaction times are required for the carbonyl-to-hydroxy reduction, however. For example, at C., about 4 to 24 hours are required; at higher temperatures, e.g., 50-60 0, about one to 2 hours are sufficient.

This carbonyl reduction usually produces a mixture of PGF a -type and PGF -type compounds, i.e., compounds with the alpha configuration and compounds with the beta configuration for the hydroxy at 09. This mixture of alpha and beta isomers is separated by methods known in the art, e.g., chromatography on silica gel. See Pike et al., ibid., for example. If the Formula-XII starting material is a mixture of Ila II- aIIB isomers, then this reduction will usually produce 26 four isomers, i.e., 9a, Ila, 9a, IIB, 9/3, Ila, and 93, 11,8. Those compounds are also separated from such mixtures by silica gel chromatography.

Regarding the transformation of XII to XIV in Chart B, it will be observed that the parameters for XII are such that all XII compounds are included in XIV. In other words, the transformation XII to XIV is an optional process step in proceeding from XII to XV. The reason for this is as follows. During the reduction of XIV to XV, the ratio of 9a-hydroxy and 9B-hydroxy compounds formed will be different when R, in XIV is hydrogen than when R is Si(A) For example, with the Formula-XIV compound wherein R is hydrogen, G is and R O- represents HO---, i.e., Ila-hydroxy, sodium borohydride reduction gives 42 parts of the corresponding Formula-XV 9a-hydroxy compound, and 58 parts of the 9B-hydroxy compound. But with the F ormula-XIV compound wherein R is hydrogen, G is and R O- represents (CI-I SiO---, sodium borohydride reduction gives parts of the corresponding Formula-XV 9a-hydroxy compound and 15 parts of the 9B-hydroxy compound. Similar differences are observed with the other isomers encompassed by Formula XIV although not necessarily in the same direction. Accordingly, whether R in Formula XIV is to be hydrogen or -Si(A) depends on the particular formula XV C-9 isomer desired and the influence of silylation on the isomer ratio. For any particular Formula-XIV starting material, the latter is readily determined by small scale reduction with and without silylation. When silylation before carbonyl reduction is indicated, largely for economic reasons, it is preferred that A be methyl, i.e., that R, be (CI-I Si.

This transformation of XII to XIV wherein R is -Si-. (A);, is carried out as described above for the transformation of hydroxy to O-Si(A) at C-l5. prior to the Chart A reactions. When R in XII is hydrogen, the COOH is also transformed in part or entirely to COO-Si(A) with prolonged silylation and excess silylating agent. It is optional in transforming XII to XIV wherein R is Si-(A) whether or not the COOH of XII is esterified to COOSi(A) When G in Formula XIV is s H ococH3 or OCOCH the acetyl is removed by alcoholysis also as described above for changing acetoxy at C-15 to hydroxy. These reactions are shown in Chart B as XV to XVI.

When R in Formula XVI is methyl andthe compound wherein R is hydrogen is desired, that methyl ester is saponified, by methods known in the art. See, for example, Just et al., J. Am. Chem. Soc. 91, 5371 (1969). This saponification also changes a C-l5 acetate to a C-l5 hydroxy.

The compounds encompassed by Formula XVI include the known compounds PGF PGF and the methyl esters of those. Also included in Formula XVI are the novel compounds I5B-PGF a B- PGF B and the methyl esters of those. All of these new and old compounds are IIa-hydroxy compounds. Also included in Formula XVI are the corresponding but novel IIB-hydroxy compounds which are also en compassed by Formula V and which are useful for the pharmacological purposes described above either as such or transformed into salts or esters as described above.

When one of these Formula-XVI compounds has the R or epi configuration for the hydroxy at C-15, and the corresponding compound with the S configuration at C-l5 is desired, or when one of these Formula-XVI compounds has the S configuration for the hydroxy at C-l5, and the corresponding compound with the R or epi configuration at C-15 is desired, those desired compounds are made by the processes of Chart C. In Chart C, R R R B, and are as defined above.

The overall process scheme of Chart C is to start with one particular C-15 isomer of a compound encompassed'by Formula XVI, i.e., either 15(8) or 15(R). The C 15 hydroxy of that isomer is oxidized to a ketonic carbonyl (XVII). Then after an optional silylation of the C-9 and C-1 1 hydroxy groups (XVIII), the C-15 carbonyl .is reduced back to a secondary hydroxy group.- That reduction produces two C-l5 hydroxy isomers, one with S configuration and one with R or epi configuration. After removal of any silyl groups, the isomers XIX and XX are separated. One of the isomers will be the same compound used as starting material (XVI). The other isomer will be the desired product. The starting meterial isomer is recycled to produce more of the desired isomer. This reaction scheme has previously been used to transform PGF to 15,8- PGF, See Pike et al., J. Org. Chem. 34, 3552 (1969).

Referring now to Chart C, starting material XVI (from CHART C (ox ida ti on) XVI XVI I (si lylation) COOR XVI I R \Q/\ i (reduction) (h drol 'si 5) HO i v CUOR XIX

H OH 'WOORZ Chart B) is a single compound, a mixture of two compounds, one with alpha and one with beta configuration at C-9, or a mixture of four compounds, i.e., 911, 11a, 9a, [1B, 9B, Ila, and 93, 11/3.

For the oxidation of XVI to XVII, any oxidizing agent can be used which will oxidize an allylic alcohol to an a,B-unsaturated ketone or aldehyde. Examples of those are 2,3-dichloro-5,6-dicyano-1,4-benzoquinone, activated manganese dioxide, or nickel peroxide (see Fieser et al., Reagents for Organic Syntheses, John Wiley & Sons, Inc., New York, N.Y., 1967, pp. 215, 637, and 731 Alternatively, these oxidations are carried out by oxygenation in the presence of the l5-hydroxyprostaglandin dehydrogenase of swine lung (see Arkiv fo'r kemi 25, 293 (1966)). These reagents are used according to procedures known in the art. See, for example, J. Biol. Chem. 239, 4097 (1964).

Regarding the transformation of XVII to XVIII in Chart C, it will be observed that the parameters for XVIII are such that all XVII compounds are included in XVIII. In other words, the transformation of XVII to XVIII is an optional process step in proceeding from XVII to XIX and XX. The reason for this is as follows. During the reduction of XVIII to XIX and XX, the ratio of XIX to XX obtained will be different when R in XVIII is hydrogen than when R is Si(A) For example, reduction of the Formula-XVIII 9oz, Ila-isomer wherein R and R are both hydrogen with zinc borohydride gives the corresponding Formula-XIX and -XX in the amounts 43 parts of XIX (R or epi configuration) and 57 parts of XX (S configuration). On the other hand, when R, in the Formula-XVIII reactant is Si- (A);,, the amounts with the same reducing agent are 27 parts of XIX and 73 parts of XX. Similar differences are observed with the other isomers encompassed by Formula XVIII although not necessarily in the same direction. Accordingly, whether R, in formula XVIII is to be hydrogen or -Si(A) depends on the particular C-l isomer desired and the influence of silylation on the isomer ratio. For any particular Formula-XVII starting material, the latter is readily determined by small scale reductions with and without silylation. When silylation before carbonyl reduction is indicated, largely for economic reasons, it is preferred that A be methyl, i.e., that R, be (Cl-I Si-.

These silylations are carried out as described above for the Chart A and Chart B silylation.

The carbonyl reduction of XVIII to XIX is carried out as described above for the transformation of PGE- type Formula xlV compounds to PGF-type Formula- XV compounds. As for those reductions, the sodium, potassium and zinc borohydrides are preferred as reducing agents, especially zinc borohydride.

When the method used to isolate the carbonyl reduction product does not remove any Si(A) groups which may be present, that is accomplished as described above for the removal of Si(A) groups from Formula-XII products (Chart A, XII to XII].

The Formula-XIX and -XX products are separated from each other by methods known in the art, for example, silica gel chromatography. See, for example, Pike et al., J. Org. Chem. 34, 3552 (1969) for this type of separation.

If one of the isomers or isomer mixtures of Formulas XIX or XX is not desired for a pharmacological use as such or transformed to esters or pharmacologically acceptable salts as described above, that isomer or isomer mixture is recycled as a Formula-XVI starting material in the processes of Chart C to produce additional of the desired isomer.

The products of Formulas XIX and XX wherein the configuration of the C-1 1 hydroxy is beta are encompassed by Formula V. The products of Formula XIX wherein the configuration of the C-] I hydroxy is alpha are encompassed by Formula VI. The intermediates of Formula XVII are encompassed by Formula Vll. Thus, all of the compounds are useful for the pharmacological purposes described above for the Formula V, VI and VII compounds. The compounds prepared as in Chart C are also useful to make the other esters and the pharmacologically acceptable salts of the Formula V, VI, and VII compounds also as described above.

There are two particular embodiments of the novel process of this invention which are especially preferred. One of those embodiments provides an optional route to PGF and starts with l5fi-PGA acetate methyl ester, the most abundant component of Plexaura homomalla (Esper), 1792, forma R. The other embodiment provides a preferred route of PGE and starts with PGA readily obtained as described above by maintaining colonies or colony pieces of Plexaura homomalla (Esper), I792, forma S in contact with water in a temperature range up to 50 C. until substantially free of PGA l5 acetate methyl ester.

The first of these embodiments is shown in Chart D, and the second is shown in Chart E. All of these Chart D and Chart E reactions and reagents for effecting them are CHART D 15B-PGA acetate methyl ester I g I (oxidation) ISB-PGA acetate methyl ester or and B 10,] l-epoxides 1 (reduction) l5B-PGE and IIBJSB-PGE- l5acetate methyl esters 1 (separation) ISB-PGE IS-acetate methyl ester I (silylation) ISB-PGE I lSi-(A) ether l5-acetate methyl ester I (reduction, hydrolysis) ISB-PGF a and ISB-PCvE IS-acetate methyl esters 1, (separation) ISB-PGF Ir IS-acetate methyl ester 1 (saponification) l Sfi-PGF a 1, (oxidation) I5'oxo-PGF a 1, (silylation) l5-oxo-PGF a 9,! l-di-Si-(A) ether 1 (reduction, hydrolysis) ISB-PGF, a and PGF (separatww l5B-PGF a For CHART E PGA;

1 (silylation) PGA l5-Si-(A) ether 1 (oxidation) PGA IS-Si-(A); ether 0: and ,B 10,1l-epoxides 1, (reduction, hydrolysis) PGE and llB-PGE l(separation) PGE Brine, herein, refers to an aqueous saturated sodium chloride solution.

The A-lX solvent system used in thin layer chromatography (TLC) is made up from ethyl acetate-acetic acid-2,2,4-trimethylpentane-water (90:20:501100) according to M. Hamberg and B. Samuelsson, J. Biol. Chem. 241, 257 (1966).

PREPARATION 1 To distinguish Plexaura homomalla (Esper), 1792, forma R from Plexaura homomalla (Esper), 1792, forma S, a TLC method is used. A specimen approximately 2 cm. in length is harvested and placed in a small vial, with a small amount of water if necessary to insure it is wet, and kept closed for 6-24 hrs. About one ml. of methanol is then added and the sample is either shaken for 2 hrs. at about 25 C. or is stored for l624 hrs. at about 10 C. A sample of the liquid (IO-21 A) is spotted on a TLC plate. It is preferred to use a fluorescent-treated silica gel plate, e.g. Uniplate Silica Gel GF (Analtech, lnc., Newark, Del.). As reference standards, spots of PGA and /3-PGA are also applied. The plate is developed in the A-IX system (Hamberg and Samuelsson, J. Biol. Chem. 241 257 (1965)). The spots are finally visualized with vanillin-phosphoric acid spray (McAleer, Arch. Biochem. E. Biophys. 66, 120 (1957)). Comparison of the unknown with the two reference spots is then made and the identity of the coral established (forma S corresponding to PGA forma R to l5B-PGA PREPARATION 2 PGA from Plexaura homomalla (Esper), 1792 forma S.

Colonies of Plexaura homomalla (Esper), 1792, forma S, collected from reefs off the north shore of Jamaica, are frozen by contact with solid carbon dioxide within 1 hour after removal from the reef waters. The frozen colonies are maintained in insulated boxes containing solid carbon dioxide (temperature below about C.) until ready for thawing. Then, the frozen colonies (700 g.) are ground to a small particle size (Waring blender) and mixed with 1500 ml. of water. The mixture is maintained about 20 hrs. at about C. with stirring. Then, the mixture is filtered through a pad of diatomaceous earth, and the filtrate is acidified with concentrated hydrochloric acid to pH about 2-3. The acidified filtrate is extracted four times with ethyl acetate. The extracts are combined, filtered, washed with brine, dried with anhydrous sodium sulfate, and evaporated under reduced pressure to give 1 l g. of oily residue.

The solid residue on the diatomaceous earth filter pad is stirred 2 hours in methanol (enough to cover said residue) at 25 C. The mixture is then filtered, and the filtrate is evaporated to give 14 g. of oily residue.

The two oily residues are combined and chromatographed on 1500 g. of acid-washed silica gel, eluting successively with 8.1 of a 25 to 65% gradientof ethyl acetate in Skellysolve B, 8 l. of a 65 to 100% gradient of ethyl acetate in Skellysolve B, and 5 l. of 2% methanol in ethyl acetate, collecting 500 ml..fractions. (Skellysolve B is a mixture of isomeric hexanes). Fractions 8-12 are combined and evaporated to 1 give a small amount of PGA containing a traceof PGA methyl ester. Fractions 15-18 are combined and evaporated to give 9.54 g. of PGA Fractions 35-40 are combined to give 0.414 g. of PGE PREPARATION 3 l5B-PGA from Plexaura Homomalla (Esper), 1792, forma R.

Colonies of Plexaura homomalla (Esper), 1792, forma R, collected from reefs off the southwest shore of Florida near Miami, are chopped into chunks several inches long. The chunks are frozen by contact with solid carbon dioxide with 1 hour after removal from the reef waters. The frozen colony pieces are maintained in insulated boxes containing solid carbon dioxide (temperature below about 20 C.) until ready for thawing. Then, colony pieces (600 g.) are mixed with 1500 ml. of water. The mixture is stirred and maintained at 25 C. for 23 hours. The mixture is then filtered through a pad of diatomaceous earth, and the filtrate is acidified to pH about 2-3 with concentrated hydrochloric acid. In acidified filtrate is extracted four times with ethyl acetate. The extracts are combined, filtered, washed with brine, dried with anhydrous sodium sultate, and evaporated to give 9.2 g. of oily residue. 4

The solid residue on the diatomaceous earth pad is stirred 15 hours in methanol (enough to cover said residue) at 25 C. The mixture is then filtered, and the filtrate is evaporated. The residue is dissolved inethyl ac etate, and the solution washed successively with 3 N hydrochloric acid and brine, dried with anhydrous sodium sulfate, and evaporated to give 5.83 g. of an oily residue.

The second oily residue and 8.2 g. of the first oily residue are combined and chromatographed on 1 kg. of acid-washed silica gel, eluting successively with 3-1. portions of 25%, 35%, 45%, 55%, and 65% ethyl acetate in Skellysolve B, collecting 500-m]. fractions. Fractions 18-22 are combined and evaporated to give 5 .54 g. of l5B-PGA Fractions 15-17 are combined and evaporated to give 1.37 g. of 15B-PGA methyl ester.

PREPARATION 4 PGA compounds from Plexaura homomalla (Esper), 1792, forma S.

Frozen colonies of Plexaura homomalla (Esper), 1792, forma S (see Preparation 2) are broken manually into pieces several cm. in length. The pieces (500 g.) are then covered with methanol and the mixture is maintained for 3 hours at 25 C. The mixture is then ground in a Waring blender and filtered, and the filtrate is evaporated under reduced pressure. The residue is dissolved in ethyl acetate, and the solution is washed successively with one N hydrochloric acid, water, and brine, dried with anhydrous sodium sulfate, and evaporated under reduced pressure. The oily residue is chromatographed or 2 kg. of acid-washed silica gel wetpacked with Skellysolve B (a mixture of isomeric hexanes), eluting with 24 l. of a 25 to ethyl acetate in Skellysolve B gradient. The fractions which contain PGA acetate methyl ester, PGA acetate, PGA methyl ester, and PGA as shown by TLC with the A-lX system are separately combined and evaporated to give those compounds.

PREPARATION 5 15B-PGA compounds from Plexaura homomalla (Esper), 1792, forma R.

Colonies of Plexaura homomalla (Esper), l792, forma R, collected from reefs off the southeast shore of Florida near Miami, are chopped into chunks several inches long. The chunks are frozen by contact with solid carbon dioxide within one hour after removal from the reef waters. The frozen colony pieces are maintained in insulated boxes containing solid carbon dioxide (temperature below about 20 C.) until the time for extraction. Then, the frozen colony pieces are ground to a small particle size (Mitts and Merrill hogger; average largest dimension about mm). The particles 1500 g.) are then stirred at high speed with 5 gallons of dichloromethane for minutes at about C. external temperature. The mixture of dichloromethane and particles is then filtered through a pad of diatomaceous earth, and the filtrate is evaporated to about a 2-liter volume at C. under reduced pressure. The liquid which remains is washed with water, dried with sodium sulfate, and evaporated at 30 C. under reduced pressure.

The oily residue (60 g.) is chromatographed on 3 kg. of silica gel wet packed in Skellysolve B (a mixture of isomeric hexanes), eluting successively with a gradient of 4 l. of Skellysolve B and 4 l. of 20% ethyl acetate in Skellysolve B, 27 l. of 20%, 18 l. of 50%, and 8 l. of 75% ethyl acetate in Skellysolve B, collecting 600-ml. fractions. Fractions 39-60 are combined and evaporated to give 24.3 g. of l5B-PGA acetate methyl ester. Between fractions 60 and 74 those fractions shown by TLC to contain l5B-PGA acetate are combined and evaporated to yield that compound. Fractions 74-76 are combined and evaporated to give 1.03 g. of 15B- PGA methyl ester. Fractions 83-91 are combined and evaporated to give 1.08 g. of l5/3-PGE lS-acetate methyl ester. Still later fractions shown by TLC to contain l5B-PGE methyl ester are combined and evaporated to yield that compound.

Detection of the respective compounds by TLC is done by methods known in the art, e.g. by spotting the extract fractions on a TLC silica gel plate alongside spots of the authentic compounds, developing the plate with the A-IX system, and observing which spots of the extract fractions correspond exactly to the spots of the authentic compounds.

Following the procedures of Preparation 5, but substituting Plexaura homomalla (Esper), 1792, forma S for the Plexaura homomalla (Esper), 1792, forma R of that example, there are obtained the corresponding compounds of l5(S) configuration, viz.: PGA acetate methyl ester, PGA acetate, PGA methyl ester, PGE l5-acetate methyl ester, and PGE methyl ester.

PREPARATlON 6 PGA and 5,6trans-PGA Separation of PGA from 5,6-trans-PGA is done on a chromatographic column using a silver-saturated ionexchange resin. Preferably a macroreticular ion exchange resin is used, e.g. a sulfonated styrenedivinylbenzene copolymer having surface area of -50 sq. m/g., 30-40% porosity, and total exchange capacity of 4.5-5.0 meq. per gram of dry resin, for example Amberlyst 15, available from Rohm and Haas Co., Philadelphia, Pa. The acid-fomi resin is packed in a column, washed with warm water, and converted to the silver form by passing a 10% silver nitrate solution through the column until the effluent shows a pH of 3.5-4.0. The column is then washed with water to remove ionic silver, and finally with denatured ethanol (Type 3A). A solution of a mixture of PGA and 5,6- trans-PGA e.g. fractions 15-18 of Preparation 2, in ethanol is charged to the column. Elution with 3A alcohol then yields fractions which are combined according to their content of 5,6-trans-PGA (faster-eluting) or PGA Testing for the presence of 5,6-trans-PGA or PGA in the eluate is conveniently done by TLC using silver nitrite-treated silica gel plates (e.g. Analtech Uniplates dipped in saturated ethanolic silver nitrate and dried) and developing with the A-IX system. R of PGA is 0.45; R, of 5,6-trans-PGA 2 is 0.50. Combined fractions are concentrated, partitioned between dichloromethane and a little water, dried over sodium sulfate, and concentrated under reduced pressure to yield the title compounds.

For quantitatively assaying the 5,6-trans-PGA content of mixtures of PGA and 5 ,6-trans-PGA a combination thin-layer-spectrophotometric assay is used. Silica gel-impregnated glass microfiber sheets (e.g. lTLC sheets of the Gelman Instrument Co., Ann Arbor, Michigan) are impregnated with silver nitrate, using 5% ethanolic silver nitrate and drying. Spots of 100 to 200 ;/.G of the PGA mixture are applied and developed in the solvent system 2,2,4-trimethylpentane:ethyl acetatezacetic acid: water (100:35:8:l0, upper phase). The sheet is dried and sprayed with Rhodamine 6G (Applied Science Co., State College, Pa) and viewed under ultraviolet light. The areas containing the cis and trans materials (R of PGA 0.6; R, of 5,6-trans-PGA =0.7) are marked, then excised and eluted with methanol 1.9 ml.) and potassium hydroxide solution (0.1 ml. of 45%). After incubation at 40 for 30 min., the respective solutions are centrifuged and analyzed spectrophotometrically at 278 nm.

Following the procedure of Preparation 6, 5,6-trans- 15,8-PGA is separated from l5/3-PGA PREPARATION 7 PGE and 5,6-trans-PGE Following the procedure of Preparation 6, PGE is separated from 5,6-trans-PGE as follows. A solution of a mixture of PGE and 5,6-trans-PGE is charged to the column. Elution with 3A alcohol yields fractions which are combined according to their content of 5,6-trans- PGE (faster eluting) or PGE Assay for 5,6-trans- PGE or PGE is done by TLC as for the PGA -type compounds above. R, of PGE is 0.13; R, of 5,6-trans- PGE is 0.17. Combined fractions are concentrated, dried over sodium sulfate, and concentrated under reduced pressure to yield the title compounds.

PREPARATION 8 PGA IS-Acetate Methyl Ester, separation from 5,6- Trans-PGA IS-Acetate Methyl Ester.

A mixture of PGA lS-acetate methyl ester and 5,6- trans-PGA l5-acetate methyl ester (1 1.0 g., :15) is dissolved in 415 ml. of a solution of methanol-wateracetic acid (-5-04) and mercuric acetate (6.1 g.), and left standing at about 25 C. for 30 min. Water (250 ml.) is added and the mixture extracted twice with 700 ml. of Skellysolve B.

The Skellysolve B phase is washed with ml. of 60% methanol, dried over sodium sulfate, and concentrated to an oil (4.35 g.) having a high content of 5,6- trans-PGA IS-acetate methyl ester. The aqueous methanol phase is acidified with 32 ml. of 6 N. hydrochloric acid and the mixture is extracted with two portions of 700 ml. of Skellysolve B. The organic phase is This mixture is stirred under nitrogen at 25 C. for 2 dried over sodium sulfate and concentrated toan oil trans-P6 and 5,6-trans-l5B-PG compounds are subjected to the same transformations as the PG and 15,8- PG compounds disclosed herein and illustrated hereafter.

EXAMPLE 1 ISB-PGA Methyl Ester A solution of 70% aqueous perchloric acid (50 drops) in 50 drops of water is added to a solution of ISB-PGA acetate methyl ester (2.0 g.) in 100 ml. of methanol. The mixture is stirred for'15 hours at 25 C. and then diluted with 80 ml. of waterLThe methanol is removed'under reduced pressure, and the aqueous residue is extracted with ethyl acetate. The extract is washed successively with water andbrine, dried with anhydrous sodium sulfate, and evaporated. The residue is chromatographed on 200 g. of silica gel, eluting with 2.5 l. of a gradient of 20-70% ethyl acetate in Skellysolve B (a mixture of isomeric hexanes), collecting l-ml. fractions. Fractions 15-19 are combined and evaporated to give 727 mg. of 15B-PGA methyl ester.

EXAMPLE 2 PGA Methyl Ester A solution of l5B-PGA methyl ester (250 mg.) in 20 ml. of anhydrous tetrahydrofuran is cooled to 0 C. in an atmosphere of nitrogen. Tributylamine (1.5 ml.) is added, and the mixture is stirred at 0 C. while adding methanesulfonyl chloride (1 ml.) dropwise. The mixture is stirred 30 minutes at 0 C. Then, ml. of water is'added, and .the mixture is allowed to warm to 25 C. and is stirred for 1 hour. The tetrahydrofuran is evaporated under reduced pressure, and the aqueous residue is extracted with ethyl acetate. The extract is washed successively with one N hydrochloric acid, water, and brine, dried with anhydrous sodium sulfate, and evaporated. The residue is chromatographed on 30 g. of silica gel, eluting with 800 ml. ofa gradient of 20-70% ethyl acetate in Skellysolve B, collecting 25-ml. fractions. Fractions 14-16 are combined and evaporated to give 58 mg. of PGA methyl ester. Fractions 12 and 13 are combined to give 49 mg. of the starting material, 158- PGA methyl ester Following the procedure of Example 2, PGA methyl ester is transformed to a mixture of PGA and 15,8- PGA methyl esters, the two compounds being separated as in Example 2.

EXAMPLE 3 PGA 15-formate and l5BPGA l5-formate A solution of sodium carbonate (50mg) in 7.5 ml. of anhydrous formic acid is added to PGA (0.25 g

hrs. The reaction mixture is concentrated under reduced pressure, taken up in benzene, and again concentra-ted under reduced pressure. The residue is chromatographed on acid-washed silica gel (e.g. Mallinckrodt Silicar CC-4), eluting with a gradient of 25-75% ethyl acetate-Skellysolve B (isomeric hexane mixture) and collecting fractions. Those fractions shown by TLC 'to contain-the respective 15-formate compound, separated from its isomer and free of starting material and impurities, are combined and concentrated under reduced pressure to give the title compounds.

EXAMPLE 4 PGA and ISB-PGA PGA l5-formate (100 mg., Example 3) is dissolved in a mixture of 10 ml. of methanol and 2.5 ml. of saturated aqueous sodium bicarbonate solution. The solution is stirred under nitrogen at 25 C. for 2.5 hrs. Then 5 ml. of water and 2 ml. of l N. hydrochloric acid are added, and the solution concentrated. The aqueous residue is adjusted to pH 2-3 and extracted three times with ethyl acetate. The combined extracts are washed with water, dried over sodium sulfate, and concentrated to yield PGA Similarly, hydrolysis of ISB-PGA l5-formate (Example 3) yields l5B-PGA with stirring to a solution of 15B-PGA acetate methyl ester (265 g.) in 5000 ml. of methanol under a nitrogen atmosphere at 20 C. Then, one N aqueous potassium hydroxide solution (50 ml.) is added gradually during one hour with stirring at 20 C. The mixture is stirred an additional 2 hours at -20 C. Then, one N hydrochloric acid ml.) is added, and the methanol is removed under reduced pressure at 35 C. The residue is dissolved in 3000 ml. of ethyl acetate, and the solution is washed 3 times with 500-ml. portions of water. The combined water washes are extracted with 300 ml. of ethyl acetate. The two ethyl acetate solutions are combined, washed with brine, dried with anhydrous sodium sulfate and evaporated to give 2.75 g. of a mixture of the alpha and beta 10,11-epoxides of l5B-PGA acetate methyl ester.

EXAMPLE 6 PGAZ 10,11-Epoxide Methyl Ester Hydrogen peroxide (0.3 ml.; 30% aqueous) and one N aqueous sodium hydroxide (0.5 ml.) are added to a solution of PGA methyl ester'(229 mg.) in 10 ml. of isopropyl alcohol at 0 C. After 2.5 hours at 0 C., 10 ml. of water and 1 ml. of one N hydrochloric acid are added, and the isopropyl alcohol is removed under reduced pressure. The residue successively with water and brine, dried with anhydrous sodium sulfate, and evaporated. The residue is chromatographed on 30 g. of silica gel, eluting with 800 ml. of a gradient of 20-70% ethyl .acetate in Skellysolve B, collecting 25- ml. fractions. Fractions 5-10 are combined and evaporated to give 136 mg. of a mixture of the alpha and beta 10,1 l-epoxides of PGA methyl ester.

EXAMPLE 7 PGA Acetate Methyl Ester a and {3 10,11-Epoxides Refer to Chart A.

A solution of PGA l5-acetate methyl ester (1.954 g.) in 30 ml. of dimethoxyethane (DME) is cooled to -55 C. under nitrogen, and 5.25 ml. of t-butyl hydroperoxide is added. Then, 5 ml. of 0.25 N. methanolic lithium hydroxide (prepared from the mono-hydrate) is added over 100 min. After about 46 hrs. an additional 2.5 ml. of the base is added over 50 min. Finally, after about 23.5 hrs. the reaction is complete, as shown by TLC. The mixture is acidified to pH 56 with 1 N hydrochloric acid and is concentrated under reduced pressure. The residue is taken up in ethyl acetate, washed with brine, dried over sodium sulfate, and concentrated under reduced pressure. The product, 2.0 g., contains the title alpha and beta compounds in a ratio of 6:1, respectively, as shown by gas chromatography.

Following the procedures of Example 7, but replacing the lithium hydroxide solution with methanolic magnesium methoxide (prepared from magnesium and anhydrous methanol), there is obtained a product containing the alpha and beta epoxides in a ratio of 4:1.

Following the procedures of Example 7, but replacing the DME with a mixture of toluene-DME (:1) and replacing the lithium hydroxide with Triton B (benzyltrimethylammonium hydroxide) in methanol, there are obtained the alpha and beta epoxides in a ratio of 7:211.

Following the procedures of Example 7, but replacing the DME with a mixture of toluene-DME (1:1) and holding the reaction temperature at 40 C., the product contains the alpha and beta epoxides in a ratio of 6:2:1.

Following the procedures of Example 7, but replacing the DME with tetrahydrofuran (THF) and replacing the lithium hydroxide solution with Triton B, there are obtained the alpha and beta epoxides in a ratio of 4:5:1.

EXAMPLE 8 ISB-PGE -Acetate Methyl Ester and 1 1,8,15,8-PGE l5-Acetate Methyl Ester Granular aluminum metal (50 g.) is added to a solution of mercuric chloride (50 g.) in 2 l. of water. The mixture is swirled until hydrogen gas evolution starts to become vigorous (about 30 seconds). Then, most of the aqueous solution is decanted, and the rest is removed by rapid filtration. The amalgamated aluminum is washed rapidly and successively with two 200-ml. portions of methanol and two 200-ml. portions of anhydrous diethyl ether. The amalgamated aluminum is then covered with anhydrous diethyl either until used.

Methanol (250 ml.) and water (25 ml.) are added to a solution of a mixture of the alpha and beta 10,11- epoxides of 15B-FGA acetate methyl ester (275 g.) in 2500 ml. of diethyl ether. The mixture is cooled to -10 C. and the amalgamated aluminum prepared as above from 50 g. of aluminum metal is added. The mixture is stirred and maintained at about 25 C. with external cooling. After 1 hour, amalgamated aluminum prepared as above from 50 g. of aluminum metal is added. After an additional hour of stirring at 25 C., amalgamated aluminum prepared as above from 50 g. of aluminum metal and also 25 ml. of water are added. After and additional hour of stirring at 25 C., g. of magnesium sulfate is added as a filter aid, and the mixture is filtered. The filter cake is washed thoroughly with dichloromethane and the combined filtrate and washings are evaporated at 25 C. under reduced pressure to give a mixture (247 g.) of 15B-PGE 15-acetate methyl ester and 11,8,15B-PGE 15-acetate methyl ester.

Part of this mixture (210 g.) is chromatographed on 30 kg. of silica gel wet-packed with 60 l. of 25% ethyl acetate in Skellysolve B (6-inch diameter column), eluting successively with 60-1. portions of 25%, 30%, 35%, 40%, 45%, 50%, 55%, and 60% ethyl acetate in Skellysolve B, collecting 4-1. fractions. Fractions 71-76 are combined and evaporated to give 27 g. of 1 13,15,8- PGE l5-acetate methyl ester. Fractions 8198 are combined and evaporated to give g. of 15B-PGE 15-Acetate Methyl Ester and IIBJSB-PGE 15Acetate Methyl Ester Anhydrous sodium acetate (0.5 g.) and zinc dust (500 mg.) are added to a solution of a mixture of the alpha and beta epoxides of 15,B-PGE acetate methyl ester, prepared as in Example 5, in 5 ml. of acetic acid. This mixture is stirred at 25 C. in an atmosphere of nitrogen and cooled to about 15 C. One-half m1. of a solution of chromium (Ill) chloride hexahydrate (300 mg.) in 1 ml. of water is added, and the mixture is stirred at 0 C. for 3 hours. The mixture is then diluted with ethyl acetate, and the solution is washed successively with four portions of water, one N hydrochloric acid, sodium bicarbonate solution, and brine, .dried with anhydrous sodium sulfate, and evaporated. The residue is chromatographed on 20 g. of silica gel, eluting with 600 m. of a gradient of 20-75% ethyl acetate in Skellysolve B, collecting 25-ml. fractions. fractions 10 and 11 are combined to give 11,8,15/3-PGE l5-acetate methyl ester. Fractions 13 and 14 are combinded to give lSfl-PGE 15-acetate methyl ester. 7 7

EXAMPLE 10 PGE Methyl Ester and l 1,8-PGE Methyl Ester Freshly prepared chromium (11) acetate (450 mg,

argon atmosphere; inorganic syntheses, 8, is added to a solution of 136 mg. of epoxides (Example 6) in a mixture of 3 ml. of acetic acid and one ml. of water in an atmosphere of argon at 0C. The mixture is stirred at 5C. under argon for 18 hours. Ice is then added to the mixture, and that mixture is extracted with ethyl acetate. The extract is washed successively with water, one N hydrochloric acid, sodium bicarbonate solution, and brine, dried with anhydrous sodium sulfate, and evaporated. The residue is chromatographed on silica gel (20 g.), eluting with 600 ml. of a gradient of 20-100% ethyl acetate in Skellysolve B, collecting 20 ml. fractions. Fractions 19-22 are combined and evaporated to give 27 mg. of 1lB-PGE methyl ester. Fractions 24-27 are combined and evaporated to give 5 mg. of PGE methyl ester.

EXAMPLE 1 l PGE and 1 lB-PGE Hydrogen peroxide (0.35 ml.; 30% aqueous) is added to a-solution of PGA (200 mg.) in 5 ml. of methanol. Themixture is cooled to -20C., and 0.75 ml. of one N aqueous sodium hydroxide solution is slowly added with stirring. After 1 'hour of stirring at 20C. one ml. of one N hydrochloric acid is added, and the mixture 

1. A COMPOUND OF THE FORMULA
 2. The compound according to claim 1 wherein R1 is methyl.
 3. The compound according to claim 1 wherein R1 is hydrogen. > 